Bear Cave sees Pheton Holdings 'being manipulated,' risk of 'collapse'
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Jul 29 2025
0mins
Stock Manipulation Concerns: The Bear Cave warns that Pheton Holdings (PTHL) is likely being manipulated by overseas groups, leading to a potential severe stock collapse due to unsubstantiated rumors of an acquisition by Gilead Sciences (GILD).
Pattern of Scams: Edwin Dorsey notes that such rumors are part of a recurring scheme where overseas scammers promote U.S.-listed Chinese companies, resulting in drastic intraday stock drops, often exceeding 90%.
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Analyst Views on GILD
Wall Street analysts forecast GILD stock price to rise
19 Analyst Rating
16 Buy
3 Hold
0 Sell
Strong Buy
Current: 125.870
Low
105.00
Averages
137.88
High
154.00
Current: 125.870
Low
105.00
Averages
137.88
High
154.00
About GILD
Gilead Sciences, Inc. is a biopharmaceutical company. It is engaged in advancing medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis, COVID-19, cancer, and inflammation. It is focused on discovering, developing, and delivering medicines to address unmet medical needs in virology, oncology, and other therapeutic areas. Its portfolio of marketed products includes AmBisome, Atripla, Biktarvy, Cayston, Complera, Descovy, Descovy for PrEP, Emtriva, Epclusa, Eviplera, Genvoya, Harvoni, Hepcludex, Hepsera, Jyseleca, Letairis, Livdelzi/Lyvdelzi, Odefsey, Sovaldi, Stribild, Sunlenca, Tecartus, Trodelvy, and others. It also sells and distributes authorized generic versions of Epclusa and Harvoni in the United States through its subsidiary, Asegua Therapeutics LLC. It has control on anitocabtagene autoleucel (anito cel), an investigational BCMA-directed CAR T cell therapy for multiple myeloma. The Company also owns an antibody-drug conjugates (ADCs) platform.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
Gilead Donates Antiviral Therapy to Uganda for Ebola Response
- Ebola Response Donation: Gilead has donated over 2,000 vials of its intravenous antiviral therapy, remdesivir, to Uganda to support the ongoing Bundibugyo virus disease outbreak response, showcasing the company's long-standing commitment to addressing emerging infectious diseases.
- Emergency Use Framework: This donation is provided under compassionate use and Monitored Emergency Use of Unregistered and Investigational Interventions (MEURI) frameworks, aimed at treating Bundibugyo virus disease patients, while Gilead is also preparing to respond to requests from the Democratic Republic of the Congo and the WHO.
- Global Health Responsibility: Over the past decade, Gilead has supported multiple filovirus outbreaks in Sub-Saharan Africa through remdesivir donations for emergency use, reflecting the company's sustained commitment to rapid response in urgent situations, even though remdesivir is not yet approved for Bundibugyo virus disease treatment.
- R&D and Investment: Gilead's global R&D and investment exceed $32 billion, focusing on developing innovative medicines to combat life-threatening diseases, including HIV, viral hepatitis, and COVID-19, highlighting its strategic significance in public health preparedness.
See More
Future Outlook for Obesity Drugs Market
- Intensifying Market Competition: At the conference in New Orleans, Eli Lilly and Novo Nordisk showcased their GLP-1 drugs, with Novo's Wegovy prescriptions exceeding 3 million within five months of launch, indicating that oral medications are attracting more consumers and could reshape the weight loss drug market.
- New Drug Development Updates: Structure Therapeutics and AstraZeneca shared mid-stage data, and if their GLP-1 drugs succeed in Phase 3 trials, they are expected to hit the market by 2029, further enriching market options and intensifying competition.
- Innovative Administration Methods: Pfizer's new drug shows potential for monthly administration, which could be more convenient than current weekly injections, while Amgen is testing a drug that could be administered monthly or quarterly, aiming to enhance patient adherence to treatment.
- Future Market Outlook: With approximately 2.5 billion people globally classified as overweight and 890 million as obese, the competition will intensify as new drugs continue to emerge, while Lilly and Novo are also working to improve insurance coverage for GLP-1 drugs, which is expected to attract more patients.
See More
Gilead Sciences Accelerates HIV Drug Access in South Africa
- Accelerated Drug Access: On June 5, 2026, Gilead Sciences praised the South African government and the Global Fund for expediting access to lenacapavir, with CEO Daniel O’Day emphasizing South Africa's critical role in global HIV efforts, showcasing the company's commitment to public health initiatives.
- Significant Clinical Trial Results: On June 2, 2026, Gilead announced Phase 3 results for Livdelzi in primary biliary cholangitis, demonstrating a significant increase in patients achieving ALP normalization after 52 weeks compared to placebo, further supporting the drug's efficacy and safety profile.
- Long-term Efficacy Analysis: In the ongoing ASSURE study, Gilead shared post hoc analysis data showing that among 50 participants, 83% achieved ALP normalization at 12 months and 74% at 24 months, indicating Livdelzi's long-term efficacy and good tolerability without treatment discontinuations due to adverse events.
- Market Potential Assessment: While Gilead is recognized as a promising investment, analysts suggest that certain AI stocks may offer greater upside potential and lower downside risk, reflecting a diversified view of investment opportunities across different sectors.
See More
US Stocks Rebound as AI Trade Continues to Gain Momentum
- Market Rebound: The S&P 500 Index rose by 0.93%, the Dow Jones Industrial Average increased by 0.89%, and the Nasdaq 100 Index climbed by 1.17%, indicating a sustained rebound in the artificial intelligence trade that boosts market confidence and investor sentiment.
- Crude Oil Price Decline: WTI crude oil prices fell by 2% to a one-week low, which lowered inflation expectations and provided support for stocks and bonds, reflecting a positive outlook for future economic growth.
- Strong China Trade Data: May exports rose by 19.4% year-on-year, exceeding expectations of 15.0%, while imports increased by 27.4%, surpassing the anticipated 26.0%, indicating positive signals for global economic recovery that could further drive market gains.
- Tech Stocks Lead Gains: Chipmakers and AI infrastructure stocks showed strong performance, with Lam Research up over 4%, and Applied Materials and KLA Corp both rising over 3%, suggesting that the recovery in the tech sector is driving overall market growth.
See More
Merck and Gilead's Combination Pill Trials Achieve Primary Endpoint
- Clinical Trial Success: Merck and Gilead's combination drug achieved its primary endpoint in the ISLEND-1 and ISLEND-2 phase 3 trials, demonstrating efficacy in HIV treatment and potentially introducing new options to the market.
- Efficacy Comparison: The combination pill proved non-inferior to existing treatments like Biktarvy and standard antiretroviral therapies, enhancing its competitive position in the HIV treatment landscape by showing effectiveness in patients with HIV-1 RNA ≥ 50 copies/mL.
- Drug Background: Islatravir, part of Merck's Idvynso, combined with Gilead's lenacapavir (Sunlenca), shows promise in virologically suppressed HIV patients, potentially transforming current treatment protocols.
- Study Termination: The companies also announced the termination of the KEYNOTE-D46/EVOKE-03 study involving Trodelvy and Keytruda based on a Data Monitoring Committee's recommendation, reflecting a cautious approach towards this combination therapy.
See More
Merck and Gilead Discontinue Joint Study of Trodelvy and Keytruda
- Study Termination Announcement: Merck and Gilead have announced the discontinuation of the Phase 3 KEYNOTE-D46/EVOKE-03 study based on recommendations from the external Data Monitoring Committee, which indicated that while there was a numerical improvement in progression-free survival (PFS), it did not reach statistical significance, suggesting insufficient efficacy of the combination therapy in the targeted patient population, potentially impacting future clinical development directions.
- Patient Impact: Approximately 620 patients were enrolled in this study, and its termination means these patients will need to reassess their treatment options, which may lower expectations for new therapies and could affect Gilead and Merck's competitive position in the lung cancer treatment market.
- Safety Assessment: The combination of Trodelvy and Keytruda did not reveal new safety signals, with the safety profile consistent with known individual agent safety, providing a foundation for future research, but also indicating limitations in the clinical application prospects of this combination therapy.
- Future Outlook: Despite the study's termination, Trodelvy remains approved in over 60 countries for treating metastatic triple-negative breast cancer, and Gilead and Merck will continue to explore other indications, aiming to maintain innovation and market leadership in cancer treatment.
See More
Gilead Donates Antiviral Therapy to Uganda for Ebola Response
- Ebola Response Donation: Gilead has donated over 2,000 vials of its intravenous antiviral therapy, remdesivir, to Uganda to support the ongoing Bundibugyo virus disease outbreak response, showcasing the company's long-standing commitment to addressing emerging infectious diseases.
- Emergency Use Framework: This donation is provided under compassionate use and Monitored Emergency Use of Unregistered and Investigational Interventions (MEURI) frameworks, aimed at treating Bundibugyo virus disease patients, while Gilead is also preparing to respond to requests from the Democratic Republic of the Congo and the WHO.
- Global Health Responsibility: Over the past decade, Gilead has supported multiple filovirus outbreaks in Sub-Saharan Africa through remdesivir donations for emergency use, reflecting the company's sustained commitment to rapid response in urgent situations, even though remdesivir is not yet approved for Bundibugyo virus disease treatment.
- R&D and Investment: Gilead's global R&D and investment exceed $32 billion, focusing on developing innovative medicines to combat life-threatening diseases, including HIV, viral hepatitis, and COVID-19, highlighting its strategic significance in public health preparedness.
See More
Future Outlook for Obesity Drugs Market
- Intensifying Market Competition: At the conference in New Orleans, Eli Lilly and Novo Nordisk showcased their GLP-1 drugs, with Novo's Wegovy prescriptions exceeding 3 million within five months of launch, indicating that oral medications are attracting more consumers and could reshape the weight loss drug market.
- New Drug Development Updates: Structure Therapeutics and AstraZeneca shared mid-stage data, and if their GLP-1 drugs succeed in Phase 3 trials, they are expected to hit the market by 2029, further enriching market options and intensifying competition.
- Innovative Administration Methods: Pfizer's new drug shows potential for monthly administration, which could be more convenient than current weekly injections, while Amgen is testing a drug that could be administered monthly or quarterly, aiming to enhance patient adherence to treatment.
- Future Market Outlook: With approximately 2.5 billion people globally classified as overweight and 890 million as obese, the competition will intensify as new drugs continue to emerge, while Lilly and Novo are also working to improve insurance coverage for GLP-1 drugs, which is expected to attract more patients.
See More
Gilead Sciences Accelerates HIV Drug Access in South Africa
- Accelerated Drug Access: On June 5, 2026, Gilead Sciences praised the South African government and the Global Fund for expediting access to lenacapavir, with CEO Daniel O’Day emphasizing South Africa's critical role in global HIV efforts, showcasing the company's commitment to public health initiatives.
- Significant Clinical Trial Results: On June 2, 2026, Gilead announced Phase 3 results for Livdelzi in primary biliary cholangitis, demonstrating a significant increase in patients achieving ALP normalization after 52 weeks compared to placebo, further supporting the drug's efficacy and safety profile.
- Long-term Efficacy Analysis: In the ongoing ASSURE study, Gilead shared post hoc analysis data showing that among 50 participants, 83% achieved ALP normalization at 12 months and 74% at 24 months, indicating Livdelzi's long-term efficacy and good tolerability without treatment discontinuations due to adverse events.
- Market Potential Assessment: While Gilead is recognized as a promising investment, analysts suggest that certain AI stocks may offer greater upside potential and lower downside risk, reflecting a diversified view of investment opportunities across different sectors.
See More
US Stocks Rebound as AI Trade Continues to Gain Momentum
- Market Rebound: The S&P 500 Index rose by 0.93%, the Dow Jones Industrial Average increased by 0.89%, and the Nasdaq 100 Index climbed by 1.17%, indicating a sustained rebound in the artificial intelligence trade that boosts market confidence and investor sentiment.
- Crude Oil Price Decline: WTI crude oil prices fell by 2% to a one-week low, which lowered inflation expectations and provided support for stocks and bonds, reflecting a positive outlook for future economic growth.
- Strong China Trade Data: May exports rose by 19.4% year-on-year, exceeding expectations of 15.0%, while imports increased by 27.4%, surpassing the anticipated 26.0%, indicating positive signals for global economic recovery that could further drive market gains.
- Tech Stocks Lead Gains: Chipmakers and AI infrastructure stocks showed strong performance, with Lam Research up over 4%, and Applied Materials and KLA Corp both rising over 3%, suggesting that the recovery in the tech sector is driving overall market growth.
See More
Merck and Gilead's Combination Pill Trials Achieve Primary Endpoint
- Clinical Trial Success: Merck and Gilead's combination drug achieved its primary endpoint in the ISLEND-1 and ISLEND-2 phase 3 trials, demonstrating efficacy in HIV treatment and potentially introducing new options to the market.
- Efficacy Comparison: The combination pill proved non-inferior to existing treatments like Biktarvy and standard antiretroviral therapies, enhancing its competitive position in the HIV treatment landscape by showing effectiveness in patients with HIV-1 RNA ≥ 50 copies/mL.
- Drug Background: Islatravir, part of Merck's Idvynso, combined with Gilead's lenacapavir (Sunlenca), shows promise in virologically suppressed HIV patients, potentially transforming current treatment protocols.
- Study Termination: The companies also announced the termination of the KEYNOTE-D46/EVOKE-03 study involving Trodelvy and Keytruda based on a Data Monitoring Committee's recommendation, reflecting a cautious approach towards this combination therapy.
See More
Merck and Gilead Discontinue Joint Study of Trodelvy and Keytruda
- Study Termination Announcement: Merck and Gilead have announced the discontinuation of the Phase 3 KEYNOTE-D46/EVOKE-03 study based on recommendations from the external Data Monitoring Committee, which indicated that while there was a numerical improvement in progression-free survival (PFS), it did not reach statistical significance, suggesting insufficient efficacy of the combination therapy in the targeted patient population, potentially impacting future clinical development directions.
- Patient Impact: Approximately 620 patients were enrolled in this study, and its termination means these patients will need to reassess their treatment options, which may lower expectations for new therapies and could affect Gilead and Merck's competitive position in the lung cancer treatment market.
- Safety Assessment: The combination of Trodelvy and Keytruda did not reveal new safety signals, with the safety profile consistent with known individual agent safety, providing a foundation for future research, but also indicating limitations in the clinical application prospects of this combination therapy.
- Future Outlook: Despite the study's termination, Trodelvy remains approved in over 60 countries for treating metastatic triple-negative breast cancer, and Gilead and Merck will continue to explore other indications, aiming to maintain innovation and market leadership in cancer treatment.
See More
